Canonical Allele Identifier: CA475204549

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704472A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68937004A>C , CM000673.2:g.68937004A>C	GRCh38
NC_000011.9:g.68704472A>C , CM000673.1:g.68704472A>C	GRCh37
NC_000011.8:g.68461048A>C	NCBI36
NG_007976.1:g.38154A>C , LRG_250:g.38154A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2524A>C MANE Select	ENSP00000255078.4:p.Arg842=
ENST00000674675.1:c.669A>C
ENST00000674878.1:c.629A>C
ENST00000675118.1:c.2012A>C
ENST00000675389.1:n.799A>C
ENST00000675615.1:c.2524A>C	ENSP00000502413.1:p.Arg842=
ENST00000675648.1:n.1899A>C
ENST00000675916.1:c.768A>C
ENST00000676173.1:n.3269A>C
ENST00000676182.1:c.955A>C
ENST00000676228.1:c.*1847A>C	ENSP00000502375.1:n.*1847A>C
ENST00000255078.7:c.2524A>C	ENSP00000255078.3:p.Arg842=
ENST00000539064.5:n.2283A>C
ENST00000543739.5:n.1517A>C
NM_002180.2:c.2524A>C , LRG_250t1:c.2524A>C	NP_002171.2:p.Arg842=
XM_005273974.2:c.1513A>C	XP_005274031.1:p.Arg505=
XM_005273975.2:c.1396A>C	XP_005274032.1:p.Arg466=
XM_011544994.1:c.1291A>C	XP_011543296.1:p.Arg431=
XR_949903.1:n.2626A>C
XM_005273975.3:c.1396A>C	XP_005274032.1:p.Arg466=
XM_017017669.2:c.1513A>C	XP_016873158.1:p.Arg505=
XM_017017670.2:c.1513A>C	XP_016873159.1:p.Arg505=
XR_949903.3:n.2622A>C
NM_002180.3:c.2524A>C MANE Select	NP_002171.2:p.Arg842=